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1.
双参属Triplostegia Wall．ex DC．由分布于东南亚地区的2个种组成，为多年生草本植物。它的归属一直存在争议，有时置于川续断科Dipsacaceae或败酱科Valerianaceae，有时单立一科，即双参科Triplostegiaceae。本研究对广义川续断目Dipsacales s．l．的21种植物(分别来自于败酱科、川续断科、双参属、刺参属Morina、广义忍冬科Caprifoliaceae s. l．、五福花科 Adoxaceae)和外类群人参Panax schin-seng Nees．的叶绿体 DNA trnL-F区进行了测序，并建立系统发育树状图。结果显示，败酱科、川续断科、双参属、刺参属和广义忍冬科的4个属(双盾木属Dipelta、虫胃实属Kolkwitzia、六道木属Abelia和北极花属Linnaea)形成
了一个单系群并得到了很强的支持(100％ bootstrap)；双参属与川续断科有更近的关系，建议作为一个亚科置于川续断科；广义忍冬科为一多系类群；而刺参属与其他广义川续断目类群之间的关系尚不能确定。 相似文献
2.
本文对肋柱花属的属下分类、系统发育和地理分布等方面进行了深入研究。文用分支系统学的方法和原理，用计算机PAUP程序处理，获得了几个最简约的支序图。 肋柱花属属于龙胆亚族辐状花冠群，在这群中，论亲缘关系它与辐花属最近，与獐牙菜属次之，而与黄秦艽属关系较远。 獐牙菜属在进化程度上较肋柱花属低，因此它被选为肋柱花属的外类群。 经过支序分析，肋柱花属的18个种根据Hennig的“共近裔性原则”可组合为三个组，其中肉质根茎组为较原始的组，肋柱花组为中级进化水平的组，合萼组是进化程度最高的组。 肋柱花属是北温带分布型的属，分布于亚洲、欧洲及北美洲，直达北极。从种的地理分布型分析，表明秦岭一横断山区是本属的起源与分化中心。 随文报道了一个新组、一个新种和一个新变种。 研究了全部种类的命名模式。 相似文献
3.
郝日明 《中国科学院研究生院学报》1997,35(6):500-510
中国种子植物特有属是局限分布于中国行政区域范围内的植物成分，就其分布特点看，集中分布于中国南部亚热带广阔区域。由于中国地域广袤，虽然大多数特有属分布在东亚自然地域范围内，但南部特有属的分布范围已进入古热带植物区的马来亚森林植物亚区的北部，而西部的特有属的分布范围已进入青藏高原地区。局限于不同地域分布的特有属，各自的起源发生、所经历的地质历史过程存在一定差别。本文以自然地理区划作为研究中国种子植物特有属分布区类型的依据，将中国特有属分布区类型划分为中国东部和中部特有分布变型、中国南部特有分布变型、中国西部特有分布变型和中国北部特有分布变型4类。其中中国南部特有分布变型所含特有属为热带区系成分，其它3个特有分布变型所含特有属为温带区系成分。这样能较客观地反映中国特有属的自然地理特征，有利于研究局部地区植物区系的地质历史演变过程。 相似文献
4.
沿阶草亚科(百合科)的花粉形态及其属间亲缘关系的探讨 总被引：1，自引：0，他引：1
本文对山麦冬属Liriope 3种、沿阶草属Ophiopogon 24种和球子草属Peliosanthes 2种植物的花粉，用扫描电镜和透射电镜观察了它们的花粉的形态以及外壁的超微结构。发现它们的花粉外壁纹饰和结构明显的可分为两类：1．皱波状类型：具穿孔类型，山麦冬属和沿阶草属大体属这一类，其外壁外层具覆盖层、柱状层和基层、内层不明显，内壁明显。 2．瘤状突起类型：球子草属大体属这一类，其瘤状突起大小不均，外壁外层无覆盖层， 柱状层为大小不均的小柱，内层不明显，内壁明显。 这表明山麦冬属和沿阶草属的关系密切，但它们与球子草属的关系则较远。本文还论述了这三属的花粉形态与外部形态之间的相关性，并讨论了这三属之间的进化关系。 山麦冬属、沿阶草属和球子草属的外壁纹饰和结构等特征均支持将这三属分成沿阶草族和球子草族的观点。 相似文献
5.
通过光学显微镜和扫描电子显微镜对黄精族trib．Polygonateae 7属79种以及相关类群12属15种
的叶下表皮形态及种皮微形态进行了观察。结果表明广义黄精族植物的叶表皮形态和种皮形态可分别
分为4种类型和6种类型。在黄精族中,鹿药属Smilacina和黄精属Polygonatum的叶表皮和种皮特征在
属内表现出一定的多样性,据此可将黄精属植物分为两类：第一类多表现为叶表皮细胞形状不规则,其垂周壁为波曲形或无皱褶但弯曲,种皮表面浅穴状;另一类叶表皮细胞形状为长方形或菱形,其垂周壁
直或无皱褶但弯曲,种皮表面具脊状突起或网状结构。其中,叶表皮细胞垂周壁无皱褶但弯曲为过渡
类型,在两类植物中均有表现。本研究结果还显示出竹根七属Disporopsis和黄精属的互叶类以及鹿药属
同具有波状垂周壁的叶表皮细胞和穴型种皮。舞鹤草属Maianthemum和鹿药属的S．stellata,S．trifolia
等的种皮特征相似。万寿竹属Disporum的叶表皮特征在属内表现得相当一致,但种皮特征在东亚分布
的种和北美分布的种之间区别明显。扭柄花属Streptopus叶表皮和种皮特征在属内没有分化。卵叶扭
柄花S．ovalis的叶表皮和种皮特征与属内其它种之间没有区别,确证了它在本属中的位置。扭柄花属、
万寿竹属、七筋菇属Clintonia与黄精族其它类群差别较大,但前两者与Uvulariaceae科的油点草属Tricyr-
tis和细钟花属Uvudaria较为接近,从而支持了Dahlgren将其移至Uvulariaceae的观点。而在与外类群的关系中,铃兰族的铃兰属Convallaria与黄精族具相近的叶表皮和种皮特征。 相似文献
6.
7.
系统报道了中国桑寄生科Loranthaceae33种5变种植物的花粉形态，并与澳大利亚
2属6种植物的花粉形态做了比较。通过光学显微镜和扫描电镜观察，国产桑寄生科花粉外壁
纹饰可明显分为两个类型:一种类型为刺状或条状纹饰，另一种为颗粒状纹饰，这与该科的鞘
花族和桑寄生族两个族相吻合。在鞘花族类型中，3合沟、钝刺状或条状纹饰的花粉是基本类
型，合半沟或孔沟形，刺状纹饰的花粉是较进化的类型;在桑寄生族类型中，等极、3合沟、
颗粒状纹饰的花粉是基本类型，异极、副合半沟-合半沟、3沟形和沟形-短沟形或沟孔形、粗
糙或模糊颗粒状纹饰的花粉是较进化类型。根据萌发孔和纹饰可将桑寄生族类型花粉分为3个
类群:类群I包括五蕊寄生属Dendrophtho、梨果寄生属Scurrula、钝果寄生属Taxillus和大苞
寄生属Tolypanthus;类群II仅包括离瓣寄生属Helixanthera;类群III也仅1属，桑寄生属Lor
anthus。在这3个类群中，类群I属于基本的类型，属间花粉差别较小，其中梨果寄生属和钝
果寄生属花粉差别最小，显示出较近的亲缘关系;类群II和类群III皆是较进化类型。 相似文献
8.
通过扫描电镜对国产水鳖科植物(包括6属13种)的种皮微形态特征进行观察，并作了系统描述。根据种皮细胞形态、外种皮表面纹饰和内种皮内层小瘤状突起的特点将水鳖科植物的种皮微形态特征划分为3种类型，即海菜花型(海菜花属)、水鳖型(水鳖属)和苦草型(苦草属、水筛属、虾子草属和黑藻属)，并作出了分属检索表。本文结果表明，种皮微形态特征可作为该科族、属以及属内种级水平分类的依据，对探讨属间关系和该科的系统发育关系亦具有重要的价值。种皮微形态特征支持Hutchinson(1959)和Eckhardt(1964)将海菜花属和水鳖属分别作为一个独立的族处理的观点。苦草属、水筛属和虾子草属种皮微形态特征的高度相似性表明它们间有密切的联系，不支持将它们置于不同亚科和族的分类处理。黑藻属虽与上述3属近缘，但其外种皮特征则较为独特，因此与水筛属放在不同族中更为合理。本文种皮微形态特征的研究结果支持iki1937)和Shaffer-Fehre(1991b)等关于水鳖科与茨藻科近缘的观点。 相似文献
9.
中国主要禾本科植物花的基本类型与系统分类 总被引：1，自引：0，他引：1
本文研究、分析了禾本科33个族、174个属(632种)的花的性状；讨论了重要性状演化
的趋势。根据花、尤其花中鳞被的比较形态，把禾本科植物的花概括为三大类型七个亚型：竹
型(包括真竹亚型，稻亚型、芦竹亚型、针茅亚型)、早熟禾型(含早熟禾亚型)和黍型(包括画眉
草亚型，真黍亚型)。其结果与花的基本类型相对应的大类群，以及与幼苗基本类型、颖果基本
类型相对应的大类群是一致的，即竹亚科、稻亚科、芦竹亚科、针茅亚科、早熟禾亚科、画眉草亚 科，黍亚科。 相似文献
10.
溥发鼎 《中国科学院研究生院学报》1991,29(5):385-393
藁本属Ligusticum L.属伞形科Umbelliferae芹亚科Apioideae Drude阿米芹族Ammineae
Koch。它在阿米芹族中，是一个较进化的类群，是介于阿米芹族与前胡族Peucedaneae DC．之间的一个过渡类型。藁本属全世界60余种。我国现知有34种，占该属种数的二分之一，其中28种及2个栽培变种为我国所特有。本文比较分析藁本属的形态学性状和孢粉学性状，以小总苞片及其相关特征作为该属次级划分的主要依据，将藁本属分为两个类群，并对该属的种类作了增补，对一些种的名称、分布作了补充修订。文中还记载了4个新种。喜马拉雅藁本L．elatum(Edgew.)C.B．Clarke和开展藁本L. thomsonii C. B. Clarke var．evolutior C. B．Clarke，系我国首次记录。 相似文献
11.
本文报道了我国忍冬科54个样品，包括12属31种植物的花粉扫描电镜观察的结果, 描述了本科各属主要代表种的花粉形态特征; 及不同种的花粉类型，为化石花粉鉴定提供参考资料, 同时根据花粉的形状、大小、萌发孔及外壁雕纹的异同，讨论本科及科以下分类群的位置和系统关系。 相似文献
12.
The Xizang (Tibetan) flora with numerous endemics is of importance in Chi-
nese flora. According to recent statistics there are in Xizang 27 genera of spermatophytes
endemic to China, being only 2.25% percent of the total number of genera in the Xizang flora.
Four of them are regarded as palaeoendemics (14.81%) and the others as neoendemics (85.19%).
These endemic genera, of 30 species and 3 varieties, belong to 17 families, of which, Umbelli-
ferae contains 6 genera, 7 species and 3 varieties; Compositae has 6 genera and 7 species, and
Gentianaceae 1 genus and 2 species. All the other families each comprises one genus with a
single species.
The cosmopolitan families together comprising 14 genera with 15 species have the highest
perecentage (52.92%) and the tropical ones (5 families, 5 genera with 5 species) come to the next
(29.42%), followed by the temperate ones (3 families, 10 genera with 10 species) (17.66%). It
shows that these endemic genera are obviously related to the tropical flora and temperate one
in essence.
According to the number of species, the genera endemic to China and occurring in Xi-
zang flora may be grouped as fallows.
Monotypic endemic ones 14 (51.85%)
Ditypic endemic ones 6 (22.22%)
Oligotypic endemic ones 4 (14.81%)
Small endemic ones 3 (11.11%)
The formation of the endemic genera is correlated with the topography, climate and en-
vironmental conditions, and they may have resulted from the diversification in geography and
climatic influence for a long time. The southeastern part of Xizang Plateau is of very diverse
ecological conditions, with the adequate precipitation, which may explain the concentration of
these endemic genera in this region.
The largest similarity coefficient (38.30%) of the genera endemic to China and occurring
in Xizang is with those in Qinghai Plateau, next, with those in Yunnan and in Sichuan pro-
vinces (both 27.60%), which shows that these endemic genera are related to the floras of the
regions mentioned above.
The difference in the horizontal distribution of these endemic genera is obviously between
the southern and northern parts of Xizang Plateau. The vertical distribution of the genera is
also rather obvious, from 800 m to 5200 m above sea level, but concentrated in the zone of 3000
m to 4500 mm. Therefore their occurrence in Xizang is not only affected by the historical
environmental conditions but also controlled by the horizontal and vertical distribution.
The origin and evolution of some endemic genera, such as Psammosilene, Parateropyrum,
Sphaerotylos, Salweenia, Ajaniopsis, Xizangia, Sinoleontopodium, are discussed in this paper.
Parateropyrum, a monotypic palaeotropic endemic, belongs to the tribe Atraphaxideae in-
cluding Atraphaxis, Calligonum and Pteropyrum. It may be a comparatively advanced group
in the tribe, and is closely related to the genus Pteropyrum which is distributed in western
Asia. The genus Parapteropyrum has possibly survived as a palaetropic-tertiary relic in this
region.
Sphaerotylos, a member of the subtribe Sphaerotylinae, the tribe Boehmerieae in the family
Urticaceae, is a comparatively primitive genus in the tribe Boehmerieae so far known. As the
other subtribes, such as Boehmerinae, Sarconchlamydinae, Orecnidinae and Maoutinae, are dis-
tributed in the tropics, rarely in the subtropics, the genus is no doubt a palaetropic -tertiary
relic.
Sinoleontopodium, belonging to the tribe lnuleae in Compositae, is also related to the ge-
nus Leontopodium. It is probable that the genus Sinoleontopodium arised later than the other.
We come to the conclusion that the southern part of Xizang Plateau is also one of thecentres of the origin and differentiation of genera endemic to China. 相似文献
13.
忍冬科的数值分类初试 总被引：1，自引：0，他引：1
徐炳声 《中国科学院研究生院学报》1983,21(1):26-33
A numerical taxonomic study of Caprifoliaceae is presented. For the sake of ana-
lyzing the resemblances between the 33 species or OUT’s selected at random from the
total 13 genera of the family, a summation of 32 characters was employed in the numeri-
cal analyses. Raw data for each character were given equal weighting by condensa-
tion in order to have adequate comparisons, and the characters were converted to 51
states, each with a new range of zero to one. Owing to the lack of sufficient data from
other lines for numerical analyses, the characters used in this study were largely mor-
phological. The estimation of the coefficient resemblance between each pair or OUT’s
was established using the association coefficient method. The resulting values com-
prise the 33×33 OUT’s basic similarity matrix. The clustering technique used was
unweighted pair-group method using arithmetic averages (UPGMA).
It can be stated that the scheme of phenetic relationships shown in the resultant
dendrogram (Fig. 1) is on the whole in accord with the concepts hold by most current
taxonomists, but with some noteworthy exceptions. If the phenon line of tribal de-
markation is drawn at the level of 0.6820, the OUT’s could be roughly divided into
five groups or tribes. The fact that the highest degree of correlation between Group
I Sambuceae and Group II Viburneae on the one hand, and the great distance between
them and the rest genera of the family on the other hand agrees well with the data
obtained from morphological (Troll and Weberling, 1966), anatomical (Wilkinson,
1949, Metcalfe and Chalk, 1950), embryological (Moissl, 1941), sereological (Hillebrand
and Fairbrother, 1970), and phytochemical (Bohm and Glennie, 1971) researches.
These two tribes are most probably members of different phylogenetic origin. Trioste-
um and Symphoricarpos both show their affinities with Leycesteria of Group V
Lonicereae instead of Group III Linnaeea or Group II Viburneae as suggested by
some taxonomists, and thus supports the opinion of Troll and Weberling (1966), who
suggested that these two genera are members of the tribe Lonicereae. The location of
the phylogenetically uncertain genus Heptacodium in the dendrogram shows its close
morphological similarity to the tribe Linnaeeae.
Because of the relatively small number of characters considered in this work, and
“taxonomic judgement” was used in selecting these characters which appeared to be
most “basic” to the classification of genera in the family, as well as the limitation of
numerical taxonomy in itself, the resultant scheme of tribal relationships presented
in this paper is by no means phylogenetic, but one that provides an excellent checkon ordinary taxonomic procedures. 相似文献
14.
本文根据植物类群的系统发育和地理分布相统一的原理,讨论了“低等”金缕梅类植物的起
源和散布。 “低等”金缕梅类植物(Endress1989a的概念)包括下列7科：昆栏树科、水青树科、连香
树科、折扇叶科、领春木科、悬铃木科和金缕梅科。 该类群共有13种分布区类型,东亚区的南部和
印度支那区的北部是它的现代分布中心;根据化石证据及原始类群和外类群的分布分析,以上地区最
有可能是这类植物的起源地。 “低等”金缕梅类植物起源的时间至少可追溯到早白垩纪巴列姆期,较可
靠的化石证据说明悬铃木类植物在早白垩纪阿尔必晚期出现,而昆栏树科、水青树科、连香树科和金
缕梅科植物的出现均不晚于晚白垩纪。 最后,从环境变迁和生物演化两个方面探讨了“低等”金缕梅类植物现代分布格局的形成原因。 相似文献
15.
一般来讲,进化学派承认分支学派对系统学的研究作出了有意义的贡献,如应用分支分析方法重建系统发育,应用共有衍征确定分类群之间的分支关系以及应用外类群方法来判断性状的极性等,都对系统学的方法有所改进。但分支学派的致命缺点是拒绝接受并系类群。我们属于进化学派,认为并系类群是可以接受的。例如,根据分子资料分析,Zabelia属可以包括于Abelia属内。Zabelia属不但在花粉上和Abelia属不同,可能由于它占有了新的生态位,获得了新的特征,如叶柄基部膨大两两联合,并宿存以保护腋芽。有理由认为它们应独立成属,并不由于Zabelia属从Abelia属分出而使后者成为一个并系类群而把它们合并。分支学派的一些学者认为生物名称作为交流的工具和生物信息储存系统应有明晰的、唯一的和稳定的特性。但具等级的林奈命名系统并不具有这些特性来命名分支和种。最后,PhyloCode被提出。PhyloCode对分支的命名方法有3种,即分支结点定义、分支基干定义和衍征定义。我们认为林奈命名系统作为传媒系统在生物学界的应用已近250年,若要废弃它而采用PhyloCode,必然会在命名方面引起一片混乱。但我们并不是说PhyloCode的拥护者所提出的建议一无是处,我们建议他们宜继续进行研究。由于应用生物学种概念于植物界产生了许多问题,因此多为植物系统学家所抛弃。分支学派的兴起,推动了系统发育种概念的提出。该概念基于3个特征,即自征、区别特征和基本排它,因此分别命名为自征种概念、特征种概念和谱系种概念。事实上,目前大多数植物系统学家仍然应用着形态–地理学种概念,但我们在划分种时,必须有尽可能多的资料,特别是要将传粉、繁育系统、分子系统学资料和形态学资料结合起来。 相似文献
16.
论胡桃科植物的地理分布 总被引：1，自引：0，他引：1
路安民 《中国科学院研究生院学报》1982,20(3):257-274
The present paper aims to discuss the geog raphical distribution of the Juglandaceae
on the basis of unity of the phylogeny and the process of dispersal in the plants.
The paper is divided into the following three parts:
1. The systematic positions and the distribution patterns of nine living genera in
the family Juglandaceae (namely, Engelhardia, Oreomunnea, Alfaroa, Pterocarya, Cyclo-
carya, Juglans, Carya, Annamocarya and Platycarya) are briefly discussed. The evolu-
tional relationships between the different genera of the Juglandaceae are elucidated. The
fossil distribution and the geological date of the plant groups are reviewed. Through
the analysis for the geographical distribution of the Juglandaceous genera, the distribu-
tion patterns may be divided as follows:
A. The tropical distribution pattern
a. The genera of tropical Asia distribution: Engelhardia, Annamocarya.
b. The genera of tropical Central America distribution: Oreomunnea, Alfaroa.
B. The temperate distribution pattern
c. The genus of disjunct distribution between Western Asia and Eastern Asia:
Pterocarya.
d. The genus of disjunct distribution between Eurasia and America: Juglans.
e. The genus of disjunct distribution between Eastern Asia and North America:
Carya.
f. The genera whose distribution is confined to Eastern Asia: Cyclocarya, Platy-
carya.
2. The distribution of species
According to Takhtajan’s view point of phytochoria, the number of species in every
region are counted. It has shown clearily that the Eastern Asian Region and the Coti-
nental South-east Asian Region are most abundant in number of genera and species. Of
the 71 living species, 53 are regional endemic elements, namely 74.6% of the total species.
The author is of the opinion that most endemic species in Eurasia are of old endemic
nature and in America of new endimic nature. There are now 7 genera and 28 species
in China, whose south-western and central parts are most abundant in species, with Pro-
vince Yunnan being richest in genera and species.
3. Discussions of the distribution patterns of the Juglandaceae
A. The centre of floristic region
B. The centre of floristic regions is determined by the following two principles: a.
A large number of species concentrate in a district, namely the centre of the majority;
b. Species of a district can reflect the main stages of the systematic evolution of the
Juglandaceae, namely the centre of diversity. It has shown clearly that the southern
part of Eastern Asian region and the northern part of Continental South-east Asian
Region (i.c. Southern China and Northern Indo-China) are the main distribution centre
of the Juglandaceae, while the southern part of Sonora Region and Caribbean Region
(i.c. South-western U.S.A., Mexico and Central America) are the secondary distribution
centre.
As far as fossil records goes, it has shown that in Tertiary period the Juglanda-
ceae were widely distributed in northern Eurasia and North America, growing not only
in Europe and the Caucasus but also as far as in Greenland and Alaska. It may be
considered that the Juglandaceae might be originated from Laurasia. According to
the analysis of distribution pattern for living primitive genus, for example, Engelhar-
dia, South-western China and Northern Indo-China may be the birthplace of the most
primitive Juglandaceous plants. It also can be seen that the primitive genera and the
primitive sections of every genus in the Juglandaceae have mostly distributed in the
tropics or subtropics. At the same time, according to the analysis of morphological cha-
racters, such as naked buds in the primitive taxa of this family, it is considered that
this character has relationship with the living conditions of their ancestors. All the
evidence seems to show that the Juglandaceae are of forest origin in the tropical moun-
tains having seasonal drying period.
B. The time of the origin
The geological times of fossil records are analyzed. It is concluded that the origin
of the Juglandaceae dates back at least as early as the Cretaceous period.
C. The routes of despersal
After the emergence of the Juglandaceous plant on earth, it had first developed and
dispersed in Southern China and Indo-China. Under conditions of the stable tempera-
ture and humidity in North Hemisphere during the period of its origin and development,
the Juglandaceous plants had rapidly developed and distributed in Eurasia and dis-
persed to North America by two routes: Europe-Greenland-North America route and
Asia-Bering Land-bridge-North America route. From Central America it later reached
South America.
D. The formaation of the modern distribution pattern and reasons for this forma-
tion.
According to the fossil records, the formation of two disjunct areas was not due to
the origin of synchronous development, nor to the parallel evolution in the two con-
tinents of Eurasia and America, nor can it be interpreted as due to result of transmis-
sive function. The modern distribution pattern has developed as a result of the tectonic
movement and of the climatic change after the Tertiary period. Because of the con-
tinental drift, the Eurasian Continent was separated from the North American Conti-
nent, it had formed a disjunction between Eurasia and North America. Especially, under
the glaciation during the Late Tertiary and Quaternary Periods, the continents in Eu-
rasia and North America were covered by ice sheet with the exception of “plant refuges”, most plants in the area were destroyed, but the southern part of Eastern Asia
remained practically intact and most of the plants including the Juglandaceae were
preserved from destruction by ice and thence became a main centre of survival in the
North Hemisphere, likewise, there is another centre of survival in the same latitude in
North America and Central America.
E. Finally, the probable evolutionary relationships of the genera of the Juglanda-ceae is presented by the dendrogram in the text. 相似文献
17.
本文结合地史初步探讨了第三纪以来武夷山苔藓植物可能发生的变化。武夷山的苔藓
植物主要为东亚区系成分和旧热带区系成分，与泛北极区系成分的相似性也相当明显。东亚
特有属(5个)系组成武夷山苔藓植物区系的重要因素之一，它低于黄山和西天目山的9个和
7个，与黄山等组成一个共同的苔藓植物东亚特有属的分布中心。从各方面的分析推测，这 类植物可能起源于第三纪，系一类“孑遗植物”。 相似文献
18.
中国及其邻近地区松杉类特有属的现代生态地理分布及其意义 总被引：1，自引：0，他引：1
1．我国及其邻近地区松杉类特有属，主要分布于我国东南部、南部和西南
部，大约相当于我国亚热带常绿阔叶林带的范围。其垂直分布一般在海拔100—
1800米之间，少数属可达2800米，但不逾越海拔3000米。
2．我国松杉类特有属分布地区的水热条件，大致为年平均温度在10℃-20℃之间，绝对最低温度为-6.3℃——11.3℃，
年降水量一般在2000毫米左右。土壤pH 4．0—5．5之间，呈酸性反应。
3．我国及其邻近地区松杉类特有属数约占全世界松杉类特有属数的37.5%，是世界上最丰富、分布最为集中的地区。这些属的化石出现于晚白垩纪或第三纪时期。 因此，我国无疑是松杉类特有属的现代地理分布中心和保存中心。这对进一步研究松杉类植物的发生和发展，具有重要的意义。 相似文献
19.
Xizang (Tibet) is rich in Leguminosae flora, comprising 41 genera and 254 species
so far known, exclusive of the commonly cultivated taxa (including 11 genera and 16
species). There are 4 endemic genera (with 8 species), 10 temperate genera (with 175
species) and 19 tropical genera (with 46 species) as well as the representatives of those
genera whose distribution centers are in East Asia-North America, Mediterranean
and Central Asia.
1. There are altogether 4 endemic genera of Leguminosae in this region. Accord-
ing to their morphological characters, systematic position and geographical distribution,
it would appear that Salweenia and Piptanthus are Tertiary paleo-endemics, while
Straceya and Cochlianths are neo-endemics. Salweenia and Piptanthus may be some
of more primitive members in the subfamily Papilionasae and their allies are largely
distributed in the southern Hemisphere. The other two genera might have been derived
from the northern temperate genus Hedysarum and the East Asian-North American
genus Apios respectively, because of their morphological resemblance. They probably
came into existanc during the uplifting of the Himalayas.
2. An analysis of temperate genera
There are twelve temperate genera of Leguminosae in the region, of which the
more important elements in composition of flora, is Astragalus, Oxytropis and Cara-
gana.
Astragalus is a cosmopolitan genus comprising 2000 species, with its center
distribution in Central Asia. 250 species, are from China so far known, in alpine zone of
Southwest and Northwest, with 70 species extending farther to the Himalayas and
Xizang Plateau.
Among them, there are 7 species (10%) common to Central Asia, 12 species (15.7%)
to Southwest China and 40 species (60%) are endemic, it indicates that the differentia-
tion of the species of the genus in the region is very active, especially in the subgenus
Pogonophace with beards in stigma. 27 species amounting to 78.5% of the total species of
the subgenus, are distributed in this region. The species in the region mainly occur in
alpine zone between altitude of 3500—300 m. above sea-level. They have developed into
a member of representative of arid and cold alpine regions.
The endemic species of Astragalus in Xizang might be formed by specialization of
the alien and native elements. It will be proved by a series of horizontal and vertical vicarism of endemic species. For example, Astragalus bomiensis and A. englerianus are
horizontal and vertical vicarism species, the former being distributed in southeast part
of Xizang and the latter in Yunnan; also A. arnoldii and A. chomutovii, the former
being an endemic on Xizang Plateau and latter in Central Asia.
The genus Oxytropis comprises 300 species which are mainly distributed in the
north temperate zone. About 100 species are from China so far known, with 40 species
extending to Himalayas and Xizang Plateau. The distribution, formation and differ-
entiation of the genus in this region are resembled to Astragalus. These two genera are
usually growing together, composing the main accompanying elements of alpine mea-
dow and steppe.
Caragana is an endemic genus in Eurasian temperate zone and one of constructive
elements of alpine bush-wood. About 100 species are from China, with 16 species in Xi-
zang. According to the elements of composition, 4 species are common to Inner Mon-
golia and Kausu, 4 species to Southwest of China, the others are endemic. This not only
indicates that the species of Caragana in Xizang is closely related to those species of
above mentioned regions, but the differentiation of the genus in the region is obviously
effected by the uplifting of Himalayas, thus leading to the formations of endemic species
reaching up to 50%.
3. An Analysis of Tropical Genera
There are 19 tropical genera in the region. They concentrate in southeast of Xizang
and southern flank of the Himalayas. All of them but Indigofera and Desmodium are
represented by a few species, especially the endemic species. Thus, it can be seen that
they are less differentiated than the temperate genera.
However, the genus Desmodium which extends from tropical southeast and northeast
Asia to Mexio is more active in differentiation than the other genera. According to Oha-
Shi,s system about the genus in 1973, the species of Desmodium distributed in Sino-Hima-
laya region mostly belong to the subgenus Dollinera and subgenus Podocarpium. The
subgenus Dollinera concentrates in both Sino-Himalaya region and Indo-China with 14
species, of which 7 species are endemic in Sino-Himalaya. They are closely related to
species of Indo-China, southern Yunnan and Assam and shows tha tthey have close con-
nections in origin and that the former might be derived from the latter.
Another subgenus extending from subtropical to temperate zone is Podocarpium.
Five out of the total eight species belonging to the subgenus are distributed in Sino-
Himalaya and three of them are endemic.
An investigation on interspecific evolutionary relationship and geographic distribu-
tion of the subgenus shows that the primary center of differentiation of Podocarpium
is in the Sino-Himalaya region.
Finally, our survey shows that owing to the uplifting of the Himalayas which has
brought about complicated geographic and climatic situations, the favorable conditions
have been provided not only for the formation of the species but also for the genus in cer-tain degree. 相似文献